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临床试验/KCT0008887
KCT0008887尚未招募Unknown

A study on the effectiveness of the mental health mobile application for high risk of depression in Perinatal women

Catholic Kwandong University International St.Mary's Hospital0 个研究点目标入组 88 人开始时间: 待定最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
88

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18(Year) 至 65(Year)(—)
性别
Female

入选标准

  • (1) a pregnant woman between the ages of 19 and 65
  • (2) having a depression score in Depression, Anxiety, Stress Scales (DASS-21) of 5 or higher, OR a score of the Edinburgh Postnatal Depression Scale (EPDS) of 9 or higher
  • (3) smartphone owners
  • (4) meet the minimum smartphone specifications

排除标准

  • (1) over 32 weeks of gestation
  • (2) being expected to give childbirth within 4 weeks (during the intervention period)
  • (3) diagnosed with bipolar or psychotic major depressive disorder
  • (4) diagnosed with Post-Traumatic Stress Disorder (PTSD) and Obstructive Compulsive Disorder (OCD) among psychiatric comorbidities

研究者

发起方
Catholic Kwandong University International St.Mary's Hospital

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